Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 55 Records) |
| Query Trace: Syndrome and FLT3[original query] |
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| Clinical Outcomes and Co-Occurring Mutations in Patients with RUNX1-Mutated Acute Myeloid Leukemia. International journal of molecular sciences 2017 Jul 18 (8): . Khan Maliha, Cortes Jorge, Kadia Tapan, Naqvi Kiran, Brandt Mark, Pierce Sherry, Patel Keyur P, Borthakur Gautam, Ravandi Farhad, Konopleva Marina, Kornblau Steven, Kantarjian Hagop, Bhalla Kapil, DiNardo Courtney |
| Telomere length is an independent prognostic marker in MDS but not in de novo AML. British journal of haematology 2017 07 178 (2): 240-249. Williams Jenna, Heppel Nicole H, Britt-Compton Bethan, Grimstead Julia W, Jones Rhiannon E, Tauro Sudhir, Bowen David T, Knapper Steven, Groves Michael, Hills Robert K, Pepper Chris, Baird Duncan M, Fegan Chr |
| Molecular Characterization of Pediatric Acute Myeloid Leukemia: Results of a Multicentric Study in Brazil. Archives of medical research 2016 11 47 (8): 656-667. Andrade Francianne Gomes, Noronha Elda Pereira, Brisson Gisele Dallapicola, Dos Santos Vicente Bueno Filipe, Cezar Ingrid Sardou, Terra-Granado Eugênia, Thuler Luiz Claudio Santos, Pombo-de-Oliveira Maria S, |
| FLT3-ITD, NPM1, and DNMT3A Gene Mutations and Risk Factors in Normal Karyotype Acute Myeloid Leukemia and Myelodysplastic Syndrome Patients in Upper Northern Thailand. Asian Pacific journal of cancer prevention : APJCP 2017 11 18 (11): 3031-3039. Mevatee Piyanan, Tantiworawit Adisak, Traisathit Patrinee, Puaninta Chaniporn, Mevatee Umnat, Angsuchawan Sirinda, Bumroongkit Kanokk |
| Idiopathic hypereosinophilia is clonal disorder? Clonality identified by targeted sequencing. PloS one 2017 12 (10): e0185602. Lee Jee-Soo, Seo Heewon, Im Kyongok, Park Si Nae, Kim Sung-Min, Lee Eun Kyoung, Kim Jung-Ah, Lee Joon-Hee, Kwon Sunghoon, Kim Miyoung, Koh Insong, Hwang Seungwoo, Park Heung-Woo, Kang Hye-Ryun, Park Kyoung Soo, Kim Ju Han, Lee Dong So |
| Genetic variations of bone marrow mesenchymal stromal cells derived from acute leukemia and myelodysplastic syndrome by targeted deep sequencing. Leukemia research 2017 Sep 62 23-28. Azuma Kenko, Umezu Tomohiro, Imanishi Satoshi, Asano Michiyo, Yoshizawa Seiichiro, Katagiri Seiichiro, Ohyashiki Kazuma, Ohyashiki Junko |
| Clinicopathologic and genetic characterization of nonacute NPM1-mutated myeloid neoplasms. Blood advances 2019 5 3 (9): 1540-1545. Patel Sanjay S, Ho Caleb, Ptashkin Ryan N, Sadigh Sam, Bagg Adam, Geyer Julia T, Xu Mina L, Prebet Thomas, Mason Emily F, Seegmiller Adam C, Morgan Elizabeth A, Steensma David P, Winer Eric S, Wong Waihay J, Hasserjian Robert P, Weinberg Olga |
Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies.
The American journal of psychiatry 2019 Mar 176 (3): 217-227. Yu Dongmei, Sul Jae Hoon, Tsetsos Fotis, Nawaz Muhammad S, Huang Alden Y, Zelaya Ivette, Illmann Cornelia, Osiecki Lisa, Darrow Sabrina M, Hirschtritt Matthew E, Greenberg Erica, Muller-Vahl Kirsten R, Stuhrmann Manfred, Dion Yves, Rouleau Guy, Aschauer Harald, Stamenkovic Mara, Schlögelhofer Monika, Sandor Paul, Barr Cathy L, Grados Marco, Singer Harvey S, Nöthen Markus M, Hebebrand Johannes, Hinney Anke, King Robert A, Fernandez Thomas V, Barta Csaba, Tarnok Zsanett, Nagy Peter, Depienne Christel, Worbe Yulia, Hartmann Andreas, Budman Cathy L, Rizzo Renata, Lyon Gholson J, McMahon William M, Batterson James R, Cath Danielle C, Malaty Irene A, Okun Michael S, Berlin Cheston, Woods Douglas W, Lee Paul C, Jankovic Joseph, Robertson Mary M, Gilbert Donald L, Brown Lawrence W, Coffey Barbara J, Dietrich Andrea, Hoekstra Pieter J, Kuperman Samuel, Zinner Samuel H, Luðvigsson Pétur, Sæmundsen Evald, Thorarensen Ólafur, Atzmon Gil, Barzilai Nir, Wagner Michael, Moessner Rainald, Ophoff Roel, Pato Carlos N, Pato Michele T, Knowles James A, Roffman Joshua L, Smoller Jordan W, Buckner Randy L, Willsey A Jeremy, Tischfield Jay A, Heiman Gary A, Stefansson Hreinn, Stefansson Kári, Posthuma Danielle, Cox Nancy J, Pauls David L, Freimer Nelson B, Neale Benjamin M, Davis Lea K, Paschou Peristera, Coppola Giovanni, Mathews Carol A, Scharf Jeremiah M, |
| The Clinical impact of PTPN11 mutations in adults with acute myeloid leukemia. Leukemia 2020 6 35 (3): 691-700. Alfayez Mansour, Issa Ghayas C, Patel Keyur P, Wang Feng, Wang Xuemei, Short Nicholas J, Cortes Jorge E, Kadia Tapan, Ravandi Farhad, Pierce Sherry, Assi Rita, Garcia-Manero Guillermo, DiNardo Courtney D, Daver Naval, Pemmaraju Naveen, Kantarjian Hagop, Borthakur Gaut |
| [Analysis of ASXL1 gene variant in patients with myelodysplastic syndrome]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 Feb 37 (2): 110-115. Chen Meiyu, Liu Jie, Chao Hongying, Qin Wei, Jiang Naike, Lu Xuzhang, Cen Ling, Jiang Yu, Cai Xiaohui, Zhang Ri, Wang Qi |
| [Analysis of RUNX1 Gene Mutation in Patients with Myelodysplastic Syndrome]. Zhongguo shi yan xue ye xue za zhi 2020 Feb 28 (1): 202-208. Cai Xiao-Hui, Chen Mei-Yu, Chao Hong-Ying, Jiang Nai-Ke, Lu Xu-Zhang, Han Wen-Min, Qin Wei, Jia Zhu-X |
| The Prognostic Ability of RAS Pathway-Related Gene Mutations in Patients with Myeloid Neoplasms Treated with Hypomethylating Agents. Acta haematologica 2021 Jul 1-11. Park Hee Sue, Son Bo Ra, Shin Kyeong Seob, Byeon Seonggyu, Kim Hee Kyung, Yang Yaewon, Jeong Yusook, Han Hye Sook, Lee Ki Hyeong, Kwon Jihy |
| [Predisposition and progression of myelodysplastic syndromes]. [Rinsho ketsueki] The Japanese journal of clinical hematology 2021 5 62 (4): 278-288. Makishima Hide |
| Analytical validation and performance characteristics of a 48-gene next-generation sequencing panel for detecting potentially actionable genomic alterations in myeloid neoplasms. PloS one 2021 4 16 (4): e0243683. Rosenthal Sun Hee, Gerasimova Anna, Ma Charles, Li Hai-Rong, Grupe Andrew, Chong Hansook, Acab Allan, Smolgovsky Alla, Owen Renius, Elzinga Christopher, Chen Rebecca, Sugganth Daniel, Freitas Tracey, Graham Jennifer, Champion Kristen, Bhattacharya Anindya, Racke Frederick, Lacbawan Felicit |
| A phase I/II study of the combination of quizartinib with azacitidine or low-dose cytarabine for the treatment of patients with acute myeloid leukemia and myelodysplastic syndrome. Haematologica 2021 4 106 (8): 2121-2130. Swaminathan Mahesh, Kantarjian Hagop M, Levis Mark, Guerra Veronica, Borthakur Gautam, Alvarado Yesid, DiNardo Courtney D, Kadia Tapan, Garcia-Manero Guillermo, Ohanian Maro, Daver Naval, Konopleva Marina, Pemmaraju Naveen, Ferrajoli Alessandra, Andreeff Michael, Jain Nitin, Estrov Zeev, Jabbour Elias J, Wierda William G, Pierce Sherry, Pinsoy Maria Rhona, Xiao Lianchun, Ravandi Farhad, Cortes Jorge |
| Genetic alterations in Thai adult patients with acute myeloid leukemia and myelodysplastic syndrome-excess blasts detected by next-generation sequencing technique. Annals of hematology 2021 Apr . Owattanapanich Weerapat, Herzig Julia, Jahn Nikolaus, Panina Ekaterina, Ruchutrakool Theera, Kungwankiattichai Smith, Issaragrisil Surapol, Döhner Hartmut, Döhner Konstan |
| FLT3-ITD Mutation and FLT3 Ligand Plasma Level Were Not Associated with One-Year Survival of Indonesian Acute Myeloid Leukemia Patients. OncoTargets and therapy 2021 14 1479-1486. Rinaldi Ikhwan, Louisa Melva, Mulya Sari Resti, Arwanih El |
| Myelodysplastic syndrome with t(6;9)(p22;q34.1)/DEK-NUP214 better classified as acute myeloid leukemia? A multicenter study of 107 cases. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2021 2 34 (6): 1143-1152. Fang Hong, Yabe Mariko, Zhang Xiaohui, Kim Young, Wu Xiaojun, Wei Peng, Chi Sunyi, Zheng Lan, Garcia-Manero Guillermo, Shao Lina, Yuan Ji, Shen Yulei, Zheng Gang, Tang Guiling, Wang Wei, Loghavi Sanam, Shen Qi, Yuan Yongzhong, He Rong, Chen Dong, Medeiros L Jeffrey, Hu Shim |
| Synaptic processes and immune-related pathways implicated in Tourette syndrome. Translational psychiatry 2021 01 11 (1): 56. Tsetsos Fotis, Yu Dongmei, Sul Jae Hoon, Huang Alden Y, Illmann Cornelia, Osiecki Lisa, Darrow Sabrina M, Hirschtritt Matthew E, Greenberg Erica, Muller-Vahl Kirsten R, Stuhrmann Manfred, Dion Yves, Rouleau Guy A, Aschauer Harald, Stamenkovic Mara, Schlögelhofer Monika, Sandor Paul, Barr Cathy L, Grados Marco A, Singer Harvey S, Nöthen Markus M, Hebebrand Johannes, Hinney Anke, King Robert A, Fernandez Thomas V, Barta Csaba, Tarnok Zsanett, Nagy Peter, Depienne Christel, Worbe Yulia, Hartmann Andreas, Budman Cathy L, Rizzo Renata, Lyon Gholson J, McMahon William M, Batterson James R, Cath Danielle C, Malaty Irene A, Okun Michael S, Berlin Cheston, Woods Douglas W, Lee Paul C, Jankovic Joseph, Robertson Mary M, Gilbert Donald L, Brown Lawrence W, Coffey Barbara J, Dietrich Andrea, Hoekstra Pieter J, Kuperman Samuel, Zinner Samuel H, Wagner Michael, Knowles James A, Jeremy Willsey A, Tischfield Jay A, Heiman Gary A, Cox Nancy J, Freimer Nelson B, Neale Benjamin M, Davis Lea K, Coppola Giovanni, Mathews Carol A, Scharf Jeremiah M, Paschou Peristera, , Barr Cathy L, Batterson James R, Berlin Cheston, Budman Cathy L, Cath Danielle C, Coppola Giovanni, Cox Nancy J, Darrow Sabrina, Davis Lea K, Dion Yves, Freimer Nelson B, Grados Marco A, Greenberg Erica, Hirschtritt Matthew E, Huang Alden Y, Illmann Cornelia, King Robert A, Kurlan Roger, Leckman James F, Lyon Gholson J, Malaty Irene A, Mathews Carol A, McMahon William M, Neale Benjamin M, Okun Michael S, Osiecki Lisa, Robertson Mary M, Rouleau Guy A, Sandor Paul, Scharf Jeremiah M, Singer Harvey S, Smit Jan H, Sul Jae Hoon, Yu Dongmei, , Aschauer Harald Aschauer Harald, Barta Csaba, Budman Cathy L, Cath Danielle C, Depienne Christel, Hartmann Andreas, Hebebrand Johannes, Konstantinidis Anastasios, Mathews Carol A, Müller-Vahl Kirsten, Nagy Peter, Nöthen Markus M, Paschou Peristera, Rizzo Renata, Rouleau Guy A, Sandor Paul, Scharf Jeremiah M, Schlögelhofer Monika, Stamenkovic Mara, Stuhrmann Manfred, Tsetsos Fotis, Tarnok Zsanett, Wolanczyk Tomasz, Worbe Yulia, , Brown Lawrence, Cheon Keun-Ah, Coffey Barbara J, Dietrich Andrea, Fernandez Thomas V, Garcia-Delgar Blanca, Gilbert Donald, Grice Dorothy E, Hagstrøm Julie, Hedderly Tammy, Heiman Gary A, Heyman Isobel, Hoekstra Pieter J, Huyser Chaim, Kim Young Key, Kim Young-Shin, King Robert A, Koh Yun-Joo, Kook Sodahm, Kuperman Samuel, Leventhal Bennett L, Madruga-Garrido Marcos, Mir Pablo, Morer Astrid, Münchau Alexander, Plessen Kerstin J, Roessner Veit, Shin Eun-Young, Song Dong-Ho, Song Jungeun, Tischfield Jay A, Willsey A Jeremy, Zinner Samuel, , Aschauer Harald, Barr Cathy L, Barta Csaba, Batterson James R, Berlin Cheston, Brown Lawrence, Budman Cathy L, Cath Danielle C, Coffey Barbara J, Coppola Giovanni, Cox Nancy J, Darrow Sabrina, Davis Lea K, Depienne Christel, Dietrich Andrea, Dion Yves, Fernandez Thomas, Freimer Nelson B, Gilbert Donald, Grados Marco A, Greenberg Erica, Hartmann Andreas, Hebebrand Johannes, Heiman Gary, Hirschtritt Matthew E, Hoekstra Pieter, Huang Alden Y, Illmann Cornelia, Jankovic Joseph, King Robert A, Kuperman Samuel, Lee Paul C, Lyon Gholson J, Malaty Irene A, Mathews Carol A, McMahon William M, Müller-Vahl Kirsten, Nagy Peter, Neale Benjamin M, Nöthen Markus M, Okun Michael S, Osiecki Lisa, Paschou Peristera, Rizzo Renata, Robertson Mary M, Rouleau Guy A, Sandor Paul, Scharf Jeremiah M, Schlögelhofer Monika, Singer Harvey S, Stamenkovic Mara, Stuhrmann Manfred, Sul Jae Hoon, Tarnok Zsanett, Tischfield Jay, Tsetsos Fotis, Willsey A Jeremy, Woods Douglas, Worbe Yulia, Yu Dongmei, Zinner Samu |
| The genetic landscape of germline DDX41 variants predisposing to myeloid neoplasms. Blood 2022 6 140 (7): 716-755. Li Peng, Brown Sara, Williams Margaret, White Thomas, Xie Wei, Cui Wei, Peker Deniz, Lei Li, Kunder Christian A, Wang Huan-You, Murray Sarah S, Vagher Jennie, Kovacsovics Tibor, Patel Jay |
| [Analysis of Gene Mutation Characteristics and Prognosis of Elderly Patients with Acute Myeloid Leukemia]. Zhongguo shi yan xue ye xue za zhi 2022 Jun 30 (3): 755-759. Zhou Nai-Cen, Li Guo-Hui, Qin Wei-Wei, Wang Wen-Qing, Guo Huai-Peng, Liu Cong, Liu |
| Genetic Characteristics According to Subgroup of Acute Myeloid Leukemia with Myelodysplasia-Related Changes. Journal of clinical medicine 2022 5 11 (9): . Kang Dain, Jung Jin, Park Silvia, Cho Byung-Sik, Kim Hee-Je, Kim Yeojae, Lee Jong-Mi, Kim Hoon Seok, Ahn Ari, Kim Myungshin, Kim Yongg |
| Sorafenib in Combination With Standard Chemotherapy for Children With High Allelic Ratio FLT3/ITD+ Acute Myeloid Leukemia: A Report From the Children's Oncology Group Protocol AAML1031. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2022 3 40 (18): 2023-2035. Pollard Jessica A, Alonzo Todd A, Gerbing Robert, Brown Patrick, Fox Elizabeth, Choi John, Fisher Brian, Hirsch Betsy, Kahwash Samir, Getz Kelly, Levine John, Brodersen Lisa Eidenschink, Loken Michael R, Raimondi Susana, Tarlock Katherine, Wood Andrew, Sung Lillian, Kolb E Anders, Gamis Alan, Meshinchi Soheil, Aplenc Richa |
| Lack of Association of FLT3 rs2504235 and Absence of SLITRK1 var321 in Patients with Tic Disorders from Guangdong Province, China. Neuropsychiatric disease and treatment 2022 2 18 155-161. Gao Ming, Lin Haisheng, Li Bingxiao, Wen Junjie, Wang Yingying, Zhang Zhanhui, Chen Wenxio |
| The FLT3 internal tandem duplication mutation at disease diagnosis is a negative prognostic factor in myelodysplastic syndrome patients. Leukemia research 2022 02 113 106790. Sumiyoshi Ritsu, Tashiro Haruko, Shirasaki Ryosuke, Matsuo Takuji, Yamamoto Tadashi, Matsumoto Kensuke, Ooi Jun, Shirafuji Nao |
| UBTF tandem duplications are rare but recurrent alterations in adult AML and associated with younger age, myelodysplasia, and inferior outcome. Blood cancer journal 2023 5 13 (1): 88. Julia-Annabell Georgi, Sebastian Stasik, Jan-Niklas Eckardt, Sven Zukunft, Marita Hartwig, Christoph Röllig, Jan Moritz Middeke, Uta Oelschlägel, Utz Krug, Tim Sauer, Sebastian Scholl, Andreas Hochhaus, Tim H Brümmendorf, Ralph Naumann, Björn Steffen, Hermann Einsele, Markus Schaich, Andreas Burchert, Andreas Neubauer, Kerstin Schäfer-Eckart, Christoph Schliemann, Stefan W Krause, Mathias Hänel, Richard Noppeney, Ulrich Kaiser, Claudia D Baldus, Martin Kaufmann, Carsten Müller-Tidow, Uwe Platzbecker, Wolfgang E Berdel, Hubert Serve, Gerhard Ehninger, Martin Bornhäuser, Johannes Schetelig, Frank Kroschinsky, Christian Thiede, |
| Gene mutation analysis using next-generation sequencing and its clinical significance in patients with myeloid neoplasm: A multi-center study from China. Cancer medicine 2023 2 . Li Junnan, Pei Li, Liang Simin, Xu Shuangnian, Wang Yi, Wang Xiao, Liao Yi, Zhan Qian, Cheng Wei, Yang Zesong, Tang Xiaoqiong, Zhang Hongbin, Xiao Qing, Chen Jianbin, Liu Lin, Wang |
| The Impact of Mutation of Myelodysplasia-Related Genes in De Novo Acute Myeloid Leukemia Carrying NPM1 Mutation. Cancers 2023 1 15 (1): . Wang Yi, Quesada Andres E, Zuo Zhuang, Medeiros L Jeffrey, Yin C Cameron, Li Shaoying, Xu Jie, Borthakur Gautam, Li Yisheng, Yang Chao, Abaza Yasmin, Gao Juehua, Lu Xinyan, You M James, Zhang Yizhuo, Lin P |
| Influence of genetic co-mutation on chemotherapeutic outcome in NPM1-mutated and FLT3-ITD wild-type AML patients. Cancer medicine 2024 8 13 (15): e70102. Quan Wu, Yujiao Zhang, Baoyi Yuan, Yun Huang, Ling Jiang, Fang Liu, Ping Yan, Jiaying Cheng, Zhiquan Long, Xuejie Jia |
| Chromothripsis in myeloid malignancies. Annals of hematology 2024 5 . Chien-Yuan Ch |
- Page last reviewed:Feb 1, 2024
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